Pyrimidine derivatives as kinase modulators and method of use

11a116 2131416 1316 16 06151615616 132n-151616 2n151616 062121212n21131413132n1516132n132n232a2a The invention provides compounds and methods for inhibition of kinases, more specifically IGF 1 R kinases. The invention also provides compounds and methods for inhibition of wildtype Abl. The invention provides compounds for modulating protein kinase enzymatic activity for modulating cellular activities such as proliferation, differentiation, programmed cell death, migration and chemoinvasion. Compounds of the invention inhibit, regulate and/or modulate kinase receptor signal transduction pathways related to the changes in cellular activities as mentioned above, and the invention includes compositions which contain these compounds, and methods of using them to treat kinase-dependent diseases and conditions. A compound of formula (I), or a pharmaceutically acceptable salt, hydrate, or prodrug thereof, wherein, V is NRR, or O-R, wherein X is H, halo, C-Calkyl, NO, mono-, di-, or tri-halo substituted methyl, NRR,. C(O)O-C-Calkyl, or N(R)-C(O)-C-Calkyl; Y is H, halo, OH, C-Calkyl, C-Calkyl-NR,R, NRR,, C-Calkoxy, -N(R)-(CH)NRR, -C(O)O-C-Calkyl, -O-(CH)-NRR, -C(O)-C-Calkyl, -C-C-alkyl-R, -O-R, -C(O)-R, -O-(CH)-R, -C(O)-NRR, -C(O)-N(R)-aryl, -C(O)-N(R)(CH)-NRR, -C(O)-N(R)-(CH)-aryl -C(O)-N(R)-(CH)-heterocyclyl; or X and Y together with the atoms to which they are attached form a 4-7 membered heterocyclyl or heteroaryl group containing one or two heteroatoms independently selected from O, N, and S. Z is H, NRR, -S-R, or -O-R